Canonical Allele Identifier: CA1729176772

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760914T= , CM000669.2:g.99760914T=	GRCh38
NC_000007.13:g.99358537T= , CM000669.1:g.99358537T=	GRCh37
NC_000007.12:g.99196473T=	NCBI36
NG_008421.1:g.28272A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1414A=	ENSP00000337915.3:p.Asn472=
ENST00000651162.1:n.756A=
ENST00000651514.1:c.1321A= MANE Select	ENSP00000498939.1:p.Asn441=
ENST00000651783.1:c.862A=	ENSP00000498924.1:p.Asn288=
ENST00000652018.1:c.1174A=	ENSP00000498733.1:p.Asn392=
ENST00000336411.6:c.1321A=	ENSP00000337915.2:p.Asn441=
ENST00000354593.6:c.871A=	ENSP00000346607.2:p.Asn291=
NM_001202855.2:c.1318A=	NP_001189784.1:p.Asn440=
NM_017460.5:c.1321A=	NP_059488.2:p.Asn441=
XM_011515841.1:c.1414A=	XP_011514143.1:p.Asn472=
XM_011515842.1:c.1411A=	XP_011514144.1:p.Asn471=
NM_017460.6:c.1321A= MANE Select	NP_059488.2:p.Asn441=
NM_001202855.3:c.1318A=	NP_001189784.1:p.Asn440=